GAMP 5 Quality Risk Management · 1 GAMP®5 Quality Risk Management Sion Wyn Conformity +[44] (0)...
Transcript of GAMP 5 Quality Risk Management · 1 GAMP®5 Quality Risk Management Sion Wyn Conformity +[44] (0)...
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GAMP5 Key Concepts
• Life Cycle Approach Within a QMS
• Scaleable Life Cycle Activities
• Process and Product Understanding
• Science-Based Quality Risk Management
• Leveraging Supplier Involvement
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Quality Risk Management
ICH Q9 definition:
“A systematic process for the assessment,
control, communication, and review of
risks”
Iterative…
Throughout life cycle
Concept to retirement
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Business and Process Understanding
• Focus on risk to Patient Safety, Product
Quality, and Data Integrity
• Focus on systems that support critical
processes
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Critical Processes
• Generate, manipulate, or control data supporting
regulatory safety and efficacy submissions
• Control critical parameters in preclinical, clinical,
development, and manufacturing
• Control or provide information for product release
• Control information required in case of product recall
• Control adverse event or complaint recording or
reporting
• Support pharmacovigilance
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Managing the Risk
• Elimination by design
• Reduction to acceptable level
• Verification that risks are managed to
an acceptable level
Most Desirable
All activities scaled according to level of risk, complexity, novelty…
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ICH Q9 Principles
“The evaluation of the risk to quality
should be based on scientific knowledge
and ultimately link to the protection of
the patient.”
“The level of effort, formality, and
documentation of the quality risk
management process should be commensurate
with the level of risk.”
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Definitions
• Harm Damage to health, including the damage that can occur from loss of product quality or availability.
• Hazard The potential source of harm.
• Risk The combination of the probability of occurrence of harm and the severity of that harm.
• Severity A measure of the possible consequences of a hazard.
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Step 1 – Initial Risk Assessment
• Based on business processes, user
requirements, regulatory requirements
and known functional areas
Relevant previous assessments?
Don’t repeat unnecessarily!
Is the system GxP regulated?
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Step 2 – Identify Functions with
GxP Impact
• Functions with impact on patient safety,
product quality, and data integrity
Refer to specifications,
system architecture,
categorisation of components
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Step 3 – Perform Functional Risk
Assessments & Identify Controls
• Assess GxP functions,
considering
– Possible hazards
– How potential harm arising from
these hazards may be controlled
or mitigated
For some functions a detailed assessmentshould be performed
Identify Appropriate Controls
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Controlling the Risk
Change the process
Change the design
Apply external procedures
More detailed rigorous specification and verification
Add new features
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Functional Risk Assessment
• Described in Appendix M3
• Identify
– Hazards and risk scenarios
– Severity – impact on safety quality or other
harm
– Probability
– Detectability
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Probability
Severity
Low
Medium
High
Lo
w
Me
diu
m
Hig
h
Class 3
Class 2
Class 1
A simple two-step process:
Plot Severity vs. Probability to obtain Risk Class
Risk Assessment Tool
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Priority 1
Priority 3
Priority 2
3
2
1
Hig
h
Mediu
m
Lo
w
Ris
k C
lass
Detectability
Plot Risk Class vs. Detectability to obtain Risk Priority
Risk Assessment Tool
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Example Risk Assessment FormProject Title / Risk Assessment Overview Project Number
Assessment Scope / Assumptions Made
Assessment of Risk MeasuresFunction Sub-function Relevance
(GxP /Business)
Risk Scenarios Probability Impact Class Detection Priority
Risk Assessment Approvedby:
Module 6 – Quality Risk Mgmt.
Slide 17
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Step 4 – Implement & Verify
Appropriate Controls
• Verification activity
should demonstrate
that the controls are
effective in performing
the required risk
reduction.
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Step 5 – Review Risks
& Monitor Controls
• Mechanism
implemented.
• Monitor controls for
effectiveness.
• Change management
to apply risk
management activities
Frequency and extent of any periodic review should be based on the level of risk
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Decisions Through the Life Cycle